A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452726



Internal ID21110279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57472401..57615500hg38UCSC Ensembl
chr10:59232161..59375260hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38143100
hg19143100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv754n223
Supporting Variantsnssv18182079
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452726
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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